A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738853



Internal ID20514824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160101173..160104965hg38UCSC Ensembl
chr3:159818960..159822752hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg383793
hg193793
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296523
Samples
Known GenesIL12A-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738853
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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